FDA 510(k) Applications Submitted by TIM REEVES

FDA 510(k) Number Submission Date Device Name Applicant
K032212 07/21/2003 KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A KYPHON, INC.
K062038 07/19/2006 X-STEN MILD TOOL KIT, MODEL MTK-0001 X-STEN CORP.


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